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Catechol → 2-(Hexyloxy)phenol

HRID 2356167
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HRID 2356167 반응식
[C:1]1([C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4])[OH:2].Br[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15].C(=O)([O-])[O-].[K+].[K+]>C(C(C)=O)C>[CH2:10]([O:2][C:1]1[CH:8]=[CH:7][CH:6]=[CH:5][C:3]=1[OH:4])[CH2:11][CH2:12][CH2:13][CH2:14][CH3:15]
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참가 물질

5

반응물 3

HCID 289CatecholHCID 81011-BromohexaneHCID 11430Potassium Carbonate

생성물 1

HCID 124137162-(Hexyloxy)phenol수율 47,696.801%

시약·촉매·용매 1

HCID 6569Methyl Ethyl Ketone용매

실험 절차

A mixture of 740 mL of methyl ethyl ketone, 120 g (1.09 mol) of catechol, 178 g (1.09 mmol) of 1-bromohexane, and 211 g (1.53 mol, 1.4 eq.) of potassium carbonate was refluxed for 25 hours. After being cooled, the mixture was filtered and the solvent was evaporated. The residue of 202 g was purified by silica-gel column chromatography and was then distilled. As a result, 101 g of a transparent liquid was obtained.

후처리

  1. temperaturewas refluxed for 25 hours
  2. temperatureAfter being cooled
  3. filtrationthe mixture was filtered
  4. customthe solvent was evaporated
  5. customThe residue of 202 g was purified by silica-gel column chromatography
  6. distillationwas then distilled

출처 및 근거

ORD 기록
ord-2b4809f9b17b4289b457701bc8bcaaee
출처 데이터셋
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07758932B2

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